Genealogical study of oculopharyngeal muscular dystrophy in France

被引:5
作者
Brunet, G
Tome, FMS
Eymard, B
Robert, JM
机构
[1] INST EUROPEEN GENOMUTAT, DEPT DEMOG & GENET, LYON, FRANCE
[2] INST EUROPEAN GENOMUTAT, F-69005 LYON, FRANCE
[3] HOP LA PITIE SALPETRIERE, INST MYOL, INSERM U153, UNITE RECH DEV PATHOL & REGENERAT NEUROMUSCULAIRE, PARIS, FRANCE
关键词
oculopharyngeal muscular dystrophy; genealogy; France;
D O I
10.1016/S0960-8966(97)00079-5
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
This work is based on 54 probands affected by oculopharyngeal muscular dystrophy (OPMD). The muscle biopsy of ail these patients showed the presence of the intranuclear inclusions, specific of this disease. The residence of the probands is concentrated in three clusters: the Paris, Marseilles and Bordeaux regions. The genealogical study was carried out on 43 probands, 10 of which did not have any ascendance in France for more than two generations. The geographic origin of the 33 patients of French descent was distributed over numerous regions, not including the Paris and Marseilles regions where many patients lived. This geographic dispersion and the rarity of common genealogies of the probands, did not suggest the existence of a recent founder effect, in contrast to what is observed in the French-Canadian community. The existence of a link between French and French-Canadian families is currently being investigated. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:S34 / S37
页数:4
相关论文
共 34 条
[1]  
BARBEAU A, 1965, P 8 C INT NEUR VIENN, V2, P257
[2]  
BARBEAU A, 1966, S PROGR MUSKELDYSTRO, P102
[3]  
BASTIAENSEN LAK, 1978, CHRONIC PROGRESSIVE, P306
[4]  
BLUMEN SC, 1993, NEUROMUSCULAR DISORD, V3, P575, DOI 10.1016/0960-8966(93)90119-5
[5]   NUCLEAR INCLUSIONS IN OCULOPHARYNGEAL MUSCULAR-DYSTROPHY IN QUEBEC [J].
BOUCHARD, JP ;
GAGNE, F ;
TOME, FMS ;
BRUNET, D .
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1989, 16 (04) :446-450
[6]   THE OCULOPHARYNGEAL MUSCULAR-DYSTROPHY LOCUS MAPS TO THE REGION OF THE CARDIAC ALPHA-MYOSIN AND BETA-MYOSIN HEAVY-CHAIN GENES ON CHROMOSOME 14Q11.2-Q13 [J].
BRAIS, B ;
XIE, YG ;
SANSON, M ;
MORGAN, K ;
WEISSENBACH, J ;
KORCZYN, AD ;
BLUMEN, SC ;
FARDEAU, M ;
TOME, FMS ;
BOUCHARD, JP ;
ROULEAU, GA .
HUMAN MOLECULAR GENETICS, 1995, 4 (03) :429-434
[7]  
BRAIS B, 1995, AM J HUM GENET, V57, P910
[8]  
BROOKE MH, 1986, CLIN VIEW NEUROMUSCU, P185
[9]  
BRUNET G, 1990, REV NEUROL, V146, P425
[10]  
CAMPANELLA G, 1975, REV NEUROL, V131, P615